• Thumbnail for Beta thalassemia
    Beta thalassemiasthalassemias) are a group of inherited blood disorders. They are forms of thalassemia caused by reduced or absent synthesis of the...
    57 KB (5,458 words) - 22:49, 19 September 2024
  • Thumbnail for Thalassemia
    TDTs include Beta-thalassemia major, nondeletional HbH disease, survived Hb Bart's disease, and severe HbE/beta-thalassemia. Thalassemias are genetic disorders...
    67 KB (7,135 words) - 20:23, 17 September 2024
  • Thumbnail for Delta-beta thalassemia
    Delta-beta thalassemia is a rare form of thalassemia in which there is a reduced production of hemoglobin subunit delta and hemoglobin subunit beta and...
    8 KB (663 words) - 20:48, 14 August 2024
  • Thumbnail for Hemoglobin subunit beta
    haemoglobin. Beta thalassemia is an inherited genetic mutation in one (Beta thalassemia minor) or both (Beta thalassemia major) of the Beta globin alleles...
    18 KB (2,398 words) - 03:47, 2 May 2024
  • Thumbnail for Alpha-thalassemia
    Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 and HBA2. Thalassemias are a group of inherited blood...
    21 KB (1,588 words) - 22:52, 19 August 2024
  • Thumbnail for Hemoglobin A
    cardiovascular deformities that could lead to cardiac failure. Beta-thalassemia (β-thalassemia) is an inherited mutation of the β-globulin gene which causes...
    17 KB (2,060 words) - 02:04, 22 June 2024
  • Sickle cell-beta thalassemia is an inherited blood disorder. The disease may range in severity from being relatively benign and like sickle cell trait...
    4 KB (341 words) - 13:46, 21 March 2024
  • blood. Hemoglobin A2 may be increased in beta thalassemia or in people who are heterozygous for the beta thalassemia gene. HbA2 exists in small amounts in...
    9 KB (1,220 words) - 16:12, 24 September 2024
  • Thumbnail for Microcytic anemia
    thalassemia or beta thalassemia, respectively. Diagnosis is made by DNA analysis for alpha thalassemia and hemoglobin analysis for beta thalassemia....
    16 KB (1,705 words) - 22:21, 26 September 2023
  • Thumbnail for Fetal hemoglobin
    adult forms of hemoglobin begin to be produced. Diseases such as beta thalassemias, which affect components of the adult hemoglobin, can delay this process...
    38 KB (4,538 words) - 23:06, 16 September 2024
  • for the treatment of sickle cell disease and transfusion-dependent beta thalassemia. It was developed by Vertex Pharmaceuticals and CRISPR Therapeutics...
    20 KB (1,447 words) - 04:01, 7 September 2024
  • Thumbnail for Transfusion-dependent anemia
    advice after experiencing symptoms of anemia. Beta-thalassemia is a genetic disease mostly caused by beta-globin gene mutations. Clinical diagnosis is...
    25 KB (2,866 words) - 08:04, 7 October 2024
  • Thumbnail for Hemoglobinopathy
    variants are HbS, HbE and HbC. The main types of thalassemia are alpha-thalassemia and beta thalassemia. The two conditions may overlap because some conditions...
    19 KB (2,206 words) - 18:01, 24 April 2024
  • name Reblozyl, is a medication used for the treatment of anemia in beta thalassemia and myelodysplastic syndromes. The US Food and Drug Administration...
    11 KB (799 words) - 20:36, 19 August 2024
  • said to be helpful in differentiating iron deficiency anemia from beta thalassemia trait. The index is calculated from the results of a complete blood...
    3 KB (293 words) - 15:06, 28 June 2023
  • Thumbnail for Anisopoikilocytosis
    to various anemias, most often; beta thalassemia major, a form of microcytic anemia. In β thalassemia major the beta hemoglobin chain is completely absent...
    2 KB (132 words) - 19:19, 1 December 2023
  • Thumbnail for Hemoglobin variants
    increased in beta thalassemia. Hemoglobin F frequently increases in individuals with sickle cell anemia and sickle cell-beta thalassemia. Individuals...
    11 KB (1,171 words) - 02:58, 18 June 2024
  • Treatment of the inherited blood disorder thalassemia depends upon the level of severity. For mild forms of the condition, advice and counseling are often...
    44 KB (4,881 words) - 19:24, 3 October 2024
  • under the brand name Zynteglo, is a gene therapy for the treatment for beta thalassemia. It was developed by Bluebird Bio and was given breakthrough therapy...
    21 KB (1,463 words) - 07:11, 6 August 2024
  • betibeglogene autotemcel (Zynteglo), which treats transfusion-dependent beta thalassemia (TDT), a rare genetic blood disorder, and has been approved for use...
    15 KB (1,409 words) - 17:40, 24 September 2024
  • commercialize medicines for various diseases including sickle cell disease, beta thalassemia, various cancers, type 1 diabetes, and cardiovascular diseases. The...
    11 KB (918 words) - 14:13, 19 April 2024
  • Thumbnail for Gregg L. Semenza
    Pennsylvania, he sequenced genes linked to the recessive genetic disorder, beta-thalassemia. Semenza subsequently completed his Pediatrics residency at Duke University...
    18 KB (1,554 words) - 14:37, 7 October 2024
  • Thumbnail for Gene therapy
    in France with beta thalassemia major had been successfully treated. Beta thalassemia major is an inherited blood disease in which beta haemoglobin is...
    176 KB (18,162 words) - 23:14, 25 September 2024
  • common in pediatric patients with homozygous sickle cell disease and beta thalassemia. Up to 30% of these children may develop splenic sequestration crisis...
    1 KB (171 words) - 06:39, 6 November 2023
  • Kalyan Mansukhbhai (2017). "Co-Inheritance of Haemoglobin D-Punjab and Beta Thalassemia - A Rare Variant". Journal of Clinical and Diagnostic Research. 11...
    32 KB (3,700 words) - 16:00, 26 September 2024
  • Thumbnail for Facies (medical)
    facies – beta thalassemia Treacher Collins syndrome – deformities of the ears, eyes, cheekbones, and chin Pitt–Hopkins syndrome Beta thalassemia is associated...
    5 KB (378 words) - 15:34, 30 March 2024
  • Thumbnail for Hemoglobin Lepore syndrome
    and hematological findings bear close resemblance to those of the beta-thalassemia trait; a blood disorder that reduces the production of the iron-containing...
    11 KB (1,230 words) - 02:11, 7 July 2024
  • alpha-thalassemia intermedia, is a disease affecting hemoglobin, the oxygen carrying molecule within red blood cells. It is a form of Alpha-thalassemia which...
    9 KB (936 words) - 14:34, 26 April 2024
  • Thumbnail for Deferasirox
    are receiving long-term blood transfusions for conditions such as beta-thalassemia and other chronic anemias. It is the first oral medication approved...
    11 KB (783 words) - 04:50, 7 September 2024
  • Thumbnail for Hemoglobin electrophoresis
    levels are typically elevated in beta-thalassemia minor and hemoglobin F may be slightly increased. In beta-thalassemia major, hemoglobin A is decreased (or...
    5 KB (540 words) - 13:30, 12 July 2024